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Medicago truncatula and Glomus intraradices gene expression in cortical cells harboring arbuscules in the arbuscular mycorrhizal symbiosis

机译:丛枝菌根共生中带有丛枝的皮质细胞中t藜和glomus intraradices基因的表达

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Background Most vascular flowering plants have the capacity to form symbiotic associations with arbuscular mycorrhizal (AM) fungi. The symbiosis develops in the roots where AM fungi colonize the root cortex and form arbuscules within the cortical cells. Arbuscules are enveloped in a novel plant membrane and their establishment requires the coordinated cellular activities of both symbiotic partners. The arbuscule-cortical cell interface is the primary functional interface of the symbiosis and is of central importance in nutrient exchange. To determine the molecular events the underlie arbuscule development and function, it is first necessary to identify genes that may play a role in this process. Toward this goal we used the Affymetrix GeneChip? Medicago Genome Array to document the M. truncatula transcript profiles associated with AM symbiosis, and then developed laser microdissection (LM) of M. truncatula root cortical cells to enable analyses of gene expression in individual cell types by RT-PCR. Results This approach led to the identification of novel M. truncatula and G. intraradices genes expressed in colonized cortical cells and in arbuscules. Within the arbuscule, expression of genes associated with the urea cycle, amino acid biosynthesis and cellular autophagy was detected. Analysis of gene expression in the colonized cortical cell revealed up-regulation of a lysine motif (LysM)-receptor like kinase, members of the GRAS transcription factor family and a symbiosis-specific ammonium transporter that is a likely candidate for mediating ammonium transport in the AM symbiosis. Conclusion Transcript profiling using the Affymetrix GeneChip? Medicago Genome Array provided new insights into gene expression in M. truncatula roots during AM symbiosis and revealed the existence of several G. intraradices genes on the M. truncatula GeneChip?. A laser microdissection protocol that incorporates low-melting temperature Steedman's wax, was developed to enable laser microdissection of M. truncatula root cortical cells. LM coupled with RT-PCR provided spatial gene expression information for both symbionts and expanded current information available for gene expression in cortical cells containing arbuscules.
机译:背景技术大多数维管束开花植物具有与丛枝菌根(AM)真菌形成共生联系的能力。共生发生在AM真菌定植于根皮层并在皮质细胞内形成丛枝的根部。丛状植物被一种新的植物膜包裹,它们的建立需要两个共生伴侣的协调细胞活动。丛状皮层细胞界面是共生的主要功能界面,在养分交换中至关重要。为了确定丛枝发育和功能的分子事件,首先必须确定在此过程中可能起作用的基因。为了实现这一目标,我们使用Affymetrix GeneChip ? Medicago Genome Array来记录与AM共生相关的t藜转录本谱,然后开发了run藜根皮层细胞的激光显微解剖(LM)以进行分析。 RT-PCR检测单个细胞类型中的基因表达结果这种方法导致鉴定了在定殖的皮质细胞和丛枝中表达的新的M. trruncatula和G. intraradices基因。在丛枝内,检测到与尿素循环,氨基酸生物合成和细胞自噬相关的基因表达。对定殖的皮质细胞中基因表达的分析显示,赖氨酸基序(LysM)受体样激酶,GRAS转录因子家族的成员和共生特异性铵转运体的上调,这可能是介导介导铵转运的可能。 AM共生。结论使用Affymetrix GeneChip ? Medicago Genome Array进行转录谱分析提供了对AM共生过程中t藜根中基因表达的新见解,并揭示了t藜基因芯片上存在几个G. intraradices基因。 >?。开发了一种结合了低熔点温度Steedman蜡的激光显微切割方案,以实现对run藜根部皮层细胞的激光显微切割。 LM与RT-PCR结合为共生体提供了空间基因表达信息,并提供了在包含丛枝的皮质细胞中可用于基因表达的扩展的当前信息。

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